Gene: LINC01505 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7020666
rs7020666
LINC01505
1 9 106163165 intron variant C/T snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs7032974
rs7032974
LINC01505
1 9 106156346 intron variant T/C snv 0.30 0.700 1.000 1 2017 2017